Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12304647
MIR196A2 ; HOXC6
0.807 0.160 12 53991163 intron variant A/C snv 0.26 6
rs4074
CXCL1
0.827 0.200 4 73870427 intron variant A/G snv 0.46 6
rs1012068
DEPDC5
0.827 0.160 22 31869917 intron variant T/G snv 0.37 5
rs1054690270
LOC101928953 ; GPT
0.827 0.160 8 144505907 frameshift variant CT/- delins 5
rs16851720
RNF7
0.827 0.120 3 141744456 intron variant A/C snv 0.21 5
rs5743314
TLR3
0.851 0.160 4 186079221 intron variant G/C;T snv 5
rs5998152
DEPDC5
0.827 0.160 22 31867176 intron variant T/C snv 0.37 5
rs843645
ACYP2
0.827 0.120 2 54247527 intron variant T/A;G snv 0.19 5
rs10433937
HSD17B13
0.882 0.080 4 87308948 intron variant T/A;C;G snv 4
rs4656942
CD244
0.851 0.160 1 160861258 intron variant G/A;C;T snv 4
rs485618
CD244
0.851 0.160 1 160830690 3 prime UTR variant T/A;C;G snv 0.54 4
rs7254880
ZNF699
0.882 0.160 19 9298599 intron variant C/G snv 0.16 4
rs10945859
PRKN
0.882 0.120 6 162721570 intron variant T/C snv 0.17 3
rs1485766
VEGFC ; LOC105377555
0.882 0.120 4 176689730 intron variant T/A;G snv 3
rs26907
RASGRF2
0.882 0.240 5 81069496 intron variant G/A;T snv 3
rs3844942 0.882 0.120 4 189571800 intergenic variant T/C snv 3
rs897206619
HFE
0.882 0.120 6 26093128 missense variant C/T snv 3.5E-05 3
rs972427414
MPO
0.882 0.120 17 58279379 missense variant A/G snv 3
rs10020432
AFP
0.925 0.080 4 73455883 3 prime UTR variant A/G snv 0.54 2
rs12104272
SCAF1
0.925 0.080 19 49644795 intron variant G/A snv 0.44 2
rs2679757
AZIN1
0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs4646038
CASP9
0.925 0.080 1 15506705 intron variant C/T snv 7.0E-06 2
rs571462252
KRT8
0.925 0.080 12 52904720 missense variant G/A snv 2
rs675520
LOC102723649 ; LOC105378018
0.925 0.080 6 137672095 non coding transcript exon variant A/G;T snv 2
rs6834059
AFP
0.925 0.080 4 73435958 intron variant C/G snv 0.23 2